Canonical Allele Identifier: PA182379
Gene: MYO3A HGNC NCBI

Linked Data

ClinVar Variation Id: 178462
ClinVar RCV Id: RCV000155210 RCV001799626
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_059129.3:p.Glu351Ala
CA182378
NM_017433.5:c.1052A>C